HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nevirapine → 11-Cyclopropyl-2,3-dichloro-5,11-dihydro-4-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nevirapine | HCID 4463 | — |
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Product | 11-Cyclopropyl-2,3-dichloro-5,11-dihydro-4-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one | HCID 19960053 | — |
Reaction Steps
A mixture of 11-cyclopropyl-5,11-dihydro-4-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one (0.5 g) and N-chlorosuccinimide (0.5 g) in carbon tetrachloride (50 mL) was heated under reflux for 6 hours. An additional 0.25 g of N-chlorosuccinimide was added and heating under reflux was continued for 4 hrs more. The mixture was filtered and the solvent was evaporated. The residue was fractionated over silica gel with ethyl acetate/hexane to give the title compound which crystallized from ethyl acetate/ethanol, m.p.>290° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05620974 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-d57e4ca2cc69482f9f8ca5ef95270913 |
| Source note | uspto-grants-1997_04 |